Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam18 |
T |
C |
8: 25,118,248 (GRCm39) |
N8S |
possibly damaging |
Het |
Ago3 |
A |
G |
4: 126,311,165 (GRCm39) |
I16T |
probably benign |
Het |
Alms1 |
C |
A |
6: 85,644,945 (GRCm39) |
|
probably benign |
Het |
Brdt |
A |
G |
5: 107,525,011 (GRCm39) |
T851A |
probably damaging |
Het |
Capn7 |
A |
T |
14: 31,081,167 (GRCm39) |
I395F |
probably damaging |
Het |
Ccbe1 |
A |
G |
18: 66,199,900 (GRCm39) |
M274T |
probably benign |
Het |
Ccdc146 |
T |
C |
5: 21,499,591 (GRCm39) |
R864G |
possibly damaging |
Het |
Ccdc17 |
G |
T |
4: 116,456,749 (GRCm39) |
|
probably benign |
Het |
Ccdc85a |
C |
A |
11: 28,533,499 (GRCm39) |
C15F |
unknown |
Het |
Cpt1c |
A |
G |
7: 44,609,345 (GRCm39) |
Y715H |
probably damaging |
Het |
Dmwd |
T |
A |
7: 18,814,620 (GRCm39) |
F423L |
probably damaging |
Het |
Dock3 |
C |
G |
9: 106,788,542 (GRCm39) |
A1598P |
probably damaging |
Het |
Ext2 |
A |
G |
2: 93,644,170 (GRCm39) |
L37P |
probably damaging |
Het |
Fam120a |
T |
C |
13: 49,045,562 (GRCm39) |
D758G |
possibly damaging |
Het |
Foxn4 |
T |
C |
5: 114,396,776 (GRCm39) |
T236A |
probably damaging |
Het |
Gm9776 |
A |
T |
13: 94,495,194 (GRCm39) |
|
probably benign |
Het |
Grik1 |
A |
T |
16: 87,803,361 (GRCm39) |
M277K |
probably damaging |
Het |
H2-T23 |
T |
A |
17: 36,341,855 (GRCm39) |
M248L |
probably benign |
Het |
Hephl1 |
A |
G |
9: 15,000,265 (GRCm39) |
F329S |
possibly damaging |
Het |
Kif13a |
G |
A |
13: 46,918,072 (GRCm39) |
|
probably benign |
Het |
Knl1 |
T |
A |
2: 118,899,425 (GRCm39) |
H375Q |
probably benign |
Het |
Lox |
A |
G |
18: 52,658,177 (GRCm39) |
F332S |
probably damaging |
Het |
Ltf |
G |
A |
9: 110,851,968 (GRCm39) |
C135Y |
probably damaging |
Het |
Madd |
A |
G |
2: 91,006,554 (GRCm39) |
Y347H |
probably damaging |
Het |
Mboat1 |
T |
C |
13: 30,422,031 (GRCm39) |
Y387H |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Naip1 |
T |
C |
13: 100,545,503 (GRCm39) |
T1342A |
probably damaging |
Het |
Naip6 |
T |
C |
13: 100,453,031 (GRCm39) |
D10G |
probably benign |
Het |
Nudt8 |
A |
G |
19: 4,052,015 (GRCm39) |
R209G |
possibly damaging |
Het |
Or4c31 |
G |
T |
2: 88,291,853 (GRCm39) |
M75I |
probably damaging |
Het |
Or56a3 |
T |
C |
7: 104,735,385 (GRCm39) |
V154A |
probably benign |
Het |
Or8k35 |
A |
T |
2: 86,424,954 (GRCm39) |
Y73N |
possibly damaging |
Het |
Orc4 |
G |
A |
2: 48,827,501 (GRCm39) |
P31S |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,213,049 (GRCm39) |
S131T |
possibly damaging |
Het |
Phactr3 |
A |
G |
2: 177,973,411 (GRCm39) |
I475V |
probably damaging |
Het |
Pip |
T |
A |
6: 41,828,819 (GRCm39) |
N121K |
probably damaging |
Het |
Pla2g4d |
T |
C |
2: 120,109,384 (GRCm39) |
R222G |
probably benign |
Het |
Rbm42 |
A |
G |
7: 30,349,152 (GRCm39) |
|
probably benign |
Het |
Sowahb |
T |
C |
5: 93,191,261 (GRCm39) |
D486G |
possibly damaging |
Het |
Svep1 |
C |
T |
4: 58,087,845 (GRCm39) |
V1745I |
possibly damaging |
Het |
Tnfsf15 |
T |
A |
4: 63,652,522 (GRCm39) |
E96D |
probably benign |
Het |
Vmn2r129 |
G |
T |
4: 156,686,692 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r71 |
T |
G |
7: 85,264,828 (GRCm39) |
Y53* |
probably null |
Het |
Wapl |
A |
G |
14: 34,451,172 (GRCm39) |
I729M |
possibly damaging |
Het |
Wrnip1 |
A |
G |
13: 32,986,744 (GRCm39) |
D175G |
probably benign |
Het |
Zscan2 |
G |
A |
7: 80,513,092 (GRCm39) |
A26T |
probably benign |
Het |
|
Other mutations in Vmn1r217 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03404:Vmn1r217
|
APN |
13 |
23,298,810 (GRCm39) |
missense |
probably benign |
0.10 |
R0147:Vmn1r217
|
UTSW |
13 |
23,298,107 (GRCm39) |
missense |
probably benign |
|
R0325:Vmn1r217
|
UTSW |
13 |
23,298,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R1249:Vmn1r217
|
UTSW |
13 |
23,298,818 (GRCm39) |
missense |
probably benign |
0.01 |
R1554:Vmn1r217
|
UTSW |
13 |
23,298,464 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1777:Vmn1r217
|
UTSW |
13 |
23,298,495 (GRCm39) |
missense |
probably benign |
0.03 |
R2061:Vmn1r217
|
UTSW |
13 |
23,298,698 (GRCm39) |
missense |
probably benign |
0.19 |
R2168:Vmn1r217
|
UTSW |
13 |
23,298,714 (GRCm39) |
nonsense |
probably null |
|
R4832:Vmn1r217
|
UTSW |
13 |
23,298,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R6500:Vmn1r217
|
UTSW |
13 |
23,298,073 (GRCm39) |
nonsense |
probably null |
|
R6623:Vmn1r217
|
UTSW |
13 |
23,298,846 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6909:Vmn1r217
|
UTSW |
13 |
23,298,108 (GRCm39) |
missense |
probably benign |
|
R7708:Vmn1r217
|
UTSW |
13 |
23,298,269 (GRCm39) |
missense |
probably benign |
0.01 |
R8223:Vmn1r217
|
UTSW |
13 |
23,298,369 (GRCm39) |
missense |
probably benign |
0.03 |
R8774:Vmn1r217
|
UTSW |
13 |
23,298,108 (GRCm39) |
missense |
probably benign |
|
R8774-TAIL:Vmn1r217
|
UTSW |
13 |
23,298,108 (GRCm39) |
missense |
probably benign |
|
R9129:Vmn1r217
|
UTSW |
13 |
23,298,876 (GRCm39) |
missense |
probably benign |
0.24 |
R9182:Vmn1r217
|
UTSW |
13 |
23,298,495 (GRCm39) |
missense |
probably benign |
0.03 |
|